Probing the ArcA regulon under aerobic/ROS conditions in Salmonella enterica serovar Typhimurium
- Eduardo H Morales†1, 3, 4,
- Bernardo Collao†1,
- Prerak T Desai2,
- Iván L Calderón1,
- Fernando Gil1,
- Roberto Luraschi1,
- Steffen Porwollik2,
- Michael McClelland2 and
- Claudia P Saavedra1Email author
© Morales et al.; licensee BioMed Central Ltd. 2013
Received: 26 February 2013
Accepted: 16 September 2013
Published: 17 September 2013
Hydrogen peroxide (H2O2) is a reactive oxygen species (ROS), which is part of the oxidative burst encountered upon internalization of Salmonella enterica serovar Typhimurium (S. Typhimurium) by phagocytic cells. It has previously been established that, the ArcAB two-component system plays a critical role in ROS resistance, but the genes regulated by the system remained undetermined to date. We therefore investigated the ArcA regulon in aerobically growing S. Typhimurium before and after exposure to H2O2 by querying gene expression and other physiological changes in wild type and ΔarcA strains.
In the ΔarcA strain, expression of 292 genes showed direct or indirect regulation by ArcA in response to H2O2, of which 141were also regulated in aerobiosis, but in the opposite direction. Gene set enrichment analysis (GSEA) of the expression data from WT and ΔarcA strains, revealed that, in response to H2O2 challenge in aerobically grown cells, ArcA down regulated multiple PEP-PTS and ABC transporters, while up regulating genes involved in glutathione and glycerolipid metabolism and nucleotide transport. Further biochemical analysis guided by GSEA results showed that deletion of arcA during aerobic growth lead to increased reactive oxygen species (ROS) production which was concomitant with an increased NADH/NAD+ ratio. In absence of ArcA under aerobic conditions, H2O2 exposure resulted in lower levels of glutathione reductase activity, leading to a decreased GSH (reduced glutathione)/GSSG (oxidized glutathione) ratio.
The ArcA regulon was defined in 2 conditions, aerobic growth and the combination of peroxide treatment and aerobic growth in S. Typhimurium. ArcA coordinates a response that involves multiple aspects of the carbon flux through central metabolism, which ultimately modulates the reducing potential of the cell.
KeywordsArcAB two-component system Oxidative stress Hydrogen peroxide resistance
Salmonella enterica serovar Typhimurium (S. Typhimurium) is a Gram-negative, facultative anaerobe and intracellular bacterium that causes gastroenteritis, bacteremia and enteric fever in the murine model . During its infective cycle, S. Typhimurium is internalized by phagocytes where it is exposed to a series of antimicrobial compounds including reactive oxygen species (ROS) which trigger the production of superoxide (O2-) by phagocytic NADPH oxidase. O2- is unstable with a half life in the order of milliseconds, and under acidic conditions, as those found within the Salmonella containing vacuole (SCV), two molecules of O2- react to generate H2O2. Additionally, the S. Typhimurium genome codes for both cytoplasmic (sodA and sodB) and periplasmic (sodCI and sodCII) superoxide dismutases, that catalyze the generation of H2O2 and molecular oxygen from O2-[3–5].
The response of the bacterium to H2O2 has been mostly related to the transcription factor OxyR , however, several studies in Escherichia coli (E. coli), S. Typhimurium, S. Enteritidis and Haemophilus influenzae indicate that the response regulator ArcA is required for H2O2 resistance [7–10]. Furthermore, in E. coli H2O2 resistance depends on the cognate sensor ArcB . The ArcAB two-component system is composed of the response regulator ArcA and the hybrid sensor kinase ArcB [11, 12]. ArcAB responds to shifts in oxygen concentration [13, 14], however, the signal that activates the system remains elusive since some studies show no correlation between ArcAB activity and the ubiquinone pool , while others indicate that the system’s activity depends on the ubiquinone and/or menaquinone pools [15–17]. Upon reduction of the redox-active cysteine residues between two monomers, ArcB undergoes autophosphorylation in an ATP-dependent intramolecular reaction at a conserved histidine residue located at position 292 [18, 19]. The signal is transferred to residues D576 and H717 of ArcB and finally to residue D54 of ArcA [12, 19, 20]. Phosphorylated ArcA (ArcA-P) forms a tretamer of dimers in a 1:1 ratio of ArcA and ArcA-P, which binds to promoter regions, thereby regulating gene expression [21, 22].
Several studies in E. coli, S. Typhimurium, H. influenzae and Shewanella oneidensis have used global gene expression profiling to determine the ArcA regulon under anaerobic conditions, showing that the effect of ArcA is pleiotropic and coordinates a response that includes changes in cellular metabolism, motility and chromosomal replication, among others [8, 10, 23–26]. In S. Typhimurium 14028s grown under anaerobic conditions, ArcA regulates either directly or indirectly more than 392 genes. Additionally, an arcA mutant has a longer doubling time than the wild type strain, lacks flagella, is non-motile and remains fully virulent .
In contrast to the vast amount of information about the role of ArcA in anaerobiosis, little is known about the genes or biochemical processes that ArcA regulates in response to H2O2. Previous studies have mainly shown that arcA or arcB mutant strains are more sensitive to the toxic compound [8–10]. One study conducted in E. coli used a proteomic approach and determined that ArcA regulates the expression of fliC, oppA and gltI in response to H2O2, while in S. Typhimurium ArcA negatively regulates ompD and ompW[27, 28]. To gain further insights into the role of ArcA in ROS resistance, we compared transcriptional changes in S. Typhimurium 14028s wild-type and ΔarcA strains with and without peroxide exposure under aerobic conditions. As expected, the ΔarcA mutation affected multiple pathways confirming that ArcA has a pleiotropic effect and plays a role as a global regulator. Interestingly, the genes regulated by ArcA in response to H2O2 differ from those regulated under anaerobic conditions . A Gene Set Enrichment Analyses using the KEGG database predicted that 10 pathways were up-regulated and 2 down-regulated by ArcA in response to H2O2 treatment in aerobiosis. Finally, biochemical analyses showed that under aerobic conditions ArcA modulates the redox potential of the cell by regulating the levels of NADH and of intracellular ROS. After H2O2 exposure under aerobic conditions, ArcA was found to regulate turnover of reduced glutathione (GSH).
Bacterial strains and growth conditions
Pre-cultures of strains 14028s wild type and ΔarcA were streaked from cryo-vials stored at −80°C onto LB agar plates and allowed to grow at 37°C for 12 h. One colony was picked and grown in a 250 ml Erlenmeyer flask containing 25 ml of LB broth for 16 h at 37°C on a rotary shaker at 200 rpm. Exactly 500 μl of the cultures were then transferred into 500 ml Erlenmeyer flasks containing 50 ml of LB broth and grown in a temperature controlled rotary shaker at 200 rpm (LSI-3016R, Labtech Shaking Incubator, Indonesia). Optical density (OD600) was measured until reaching the desired OD600 for treatment with H2O2 (~ 0.4, corresponding to an incubation time of about 2.5 h). These conditions closely resemble those used in a previous study with E. coli, where 50 ml of culture grown at 200 rpm in a shaking incubator at 37°C to an OD546 of ~ 0.4 exhibited a pO2 of ≥ 90% . Solid media contained agar (20 g l-1), and plates were incubated at 37°C. When necessary, growth media was supplemented with the appropriate antibiotics.
Overnight cultures of strains 14028s and ΔarcA were diluted (1:100) and cells were grown to OD600 ~ 0.4 as described. At this point, H2O2 (1 mM) was added and cells were grown for 20 min. Control cells received no treatment. Experiments were performed in triplicate on different days. After exposure to the toxic compound, 5 ml of ice cold 5% (v/v) phenol pH 4.3 / 95% (v/v) ethanol was added to 25 ml of culture and left on ice for 20 min. Subsequently, 8 ml of this solution were centrifuged for 10 min at 8000 rpm, the supernatant was removed and the bacterial pellet was resuspended with 200 μl of 10 mM Tris–HCl (pH 8.0) that included 4 μl of lysozyme (50 mg/ml). The reaction was incubated for 10 min at 37°C, and total RNA was extracted using the High Pure RNA Isolation kit (Roche) following the manufacturer’s instructions. RNA was eluted in 105 μl of water and treated with DNaseI (Roche) at 37°C for 30 min. Total RNA was recovered using the Qiagen RNeasy kit (Qiagen), following the manufacturer’s instructions. RNA was eluted in 80 μl and subjected to a second round of DNaseI treatment (Ambion Turbo DNA-free kit) at 37°C for 30 min, purified, recovered using the Qiagen RNeasy kit (Qiagen) following the manufacturer’s instructions and eluted in 55 μl of water.
Exactly 20 μg of total RNA were used for labeling with Cy3 or Cy5. Briefly, the RNA volume was adjusted to 30 μl, 2 μl of random hexamers N6 (Sigma, 2 μg/μl) were added and the mixture was incubated for 10 min at 70°C. Subsequently, cDNA was generated using Superscript II (Invitrogen) following the manufacturer’s instructions. Final nucleotide concentrations of the reaction were 0.5 mM dATP, dTTP, dGTP and 0.2 mM dCTP. After addition of the master mix, 4 μl of 5 mM dye labeled dCTP (Cy3 or Cy5) were added to the reaction and the mixture was incubated at 42°C for 60 min. After this time, 2 μl of Superscript II were added and the reaction was incubated at 42°C for an additional 60 min. The reaction was stopped by adding 3 μl of 1 M NaOH and incubating at 70°C for 10 min. The pH was neutralized by adding 3 μl of 1 M HCl. The labeled cDNA was purified using the Qiagen PCR purification kit following the manufacturer’s instructions. The purified labeled cDNA (4 μg) was hybridized to a ~ 387.000 50-mer NimbleGen microarray (Roche NimbleGen), tiling the S. Typhimurium 14028s genome at overlapping intervals of about 12 bases on both strands, as previously described .
Data acquisition and analysis
Arrays were scanned using a GenePix 4000B laser scanner (Molecular Devices, Sunnyvale, California) at 5 μm resolution. Signal intensities were quantified using NimbleScan software v2.4 (Roche NimbleGen). Intensity values were background subtracted, normalized within (median) and between (quantile) the arrays using WebarrayDB , and converted to log2 values. For each array, the background was calculated as follows: log2 median intensity value for negative control probes + (3 * log2 intensity value standard deviation negative control probes). Negative control probes correspond to the probes located on the non-coding strand of each gene in the array. Genes with intensity values over the background were included in the analysis. After array data acquisition and normalization, two-way ANOVA was performed using MeV TM4 software , to determine uncorrected p-values. For the analysis, two categories were considered (genotype and treatment), each with two sub-categories. False Discovery Rate (FDR) adjusted q values were calculated using QVALUE in Bioconductor . Genes with a q value ≤ 0.05 for interaction and a ratio of ≥ 2 between the fold change of strains 14028s wild type and ΔarcA ((wild type treated/wild type control)/(ΔarcA treated/ ΔarcA control)) were considered to be differentially regulated in response to H2O2. Genes with a q-value of ≤ 0.05 for genotype and a fold change of ≥ 2 between strains ΔarcA and wild type (ΔarcA control/wild type control) without treatment were considered to be differentially regulated in aerobiosis. The microarray data has been deposited in GEO (http://www.ncbi.nlm.nih.gov/geo/) and is accessible via GEO Accession Number GSE34134.
Prediction of metabolic pathways altered in the different strains by treatment with H2O2 or due to the mutation of arcA was performed using the software Gene Set Enrichment Analysis (GSEA) , with the KEGG database for S. Typhimurium LT2 as a reference. Briefly, GSEA is a computational method that determines whether an a priori defined set of genes shows statistically significant, concordant differences between two biological states . To determine the pathways regulated by ArcA in response to H2O2, the log2 values of all replicas were averaged and treated as follows: (log2 14028s wild type H2O2 aerobic - log2 14028s wild type aerobic) - (log2 ΔarcA H2O2 aerobic - log2 ΔarcA aerobic). Positive Normalized Enrichment Score (NES) values represent pathways up-regulated by ArcA, while negative NES values represent pathways negatively regulated upon H2O2 treatment under aerobic conditions. To determine the pathways regulated under aerobic conditions, the log2 values of all replicas of untreated cells were averaged and treated as follows: (log2 ΔarcA aerobic - log2 14028s wild type aerobic). Pathways with an FDR of ≤ 0.25 as determined by GSEA were considered to present significant changes.
Real time quantitative RT-PCR
qRT-PCR was performed using the primers listed in Additional file 1: Table S1 as previously described , with a minor modification of the PCR program. Briefly, relative quantification was performed using Brilliant II SYBR Green QPCR Master Reagent Kit and the M×3000P detection system (Stratagene). 16S rRNA was used for normalization. The reaction mixture was carried out in a final volume of 20 μl containing 1 μl of diluted cDNA (1:1000), 0.24 μl of each primer (120 nM), 10 μl of 2 × Master Mix, 0.14 μl of diluted ROX (1:200) and 8.38 μl of H2O. The reaction was performed under the following conditions: 10 min at 95°C followed by 40 cycles of 30 s at 95°C, 30 s at 58°C and 30 s at 72°C. Finally, a melting cycle from 65°C to 95°C was performed to check for amplification specificity. Amplification efficiency was calculated from a standard curve constructed by amplifying serial dilutions of RT-PCR products for each gene. These values were used to obtain the fold-change in expression for the gene of interest normalized with 16S levels according to Pfaffl .
A positional weight matrix was generated using the ArcA-binding sites predicted in E. coli for which footprinting experiments are available reviewed in . Additionally, the binding sites predicted for members of the ArcA regulon in S. Typhimurium 14028s in anaerobiosis were also included , as was that of the ompW promoter region, which was shown to be functional . The upstream sequences of the genes regulated by ArcA in response to aerobiosis or H2O2 exposure under aerobic conditions (Additional file 2: Table S2) were retrieved (positions −400 to −1 with respect to the translation start site) from the sequenced and annotated genome of S. Typhimurium 14028s . Promoter regions with less than 20 nt between the translation start site of the ORF under analysis and the end or start of the upstream ORF were not included in the analysis. Binding sites at the promoter regions of genes regulated by ArcA in response to aerobiosis or H2O2 exposure under aerobic conditions (Additional file 2: Table S2) were predicted using the Matrix-scan software  available at http://rsat.ulb.ac.be/. The parameters used for the analysis were those given by default by the software. Binding sites with a p-value of ≤ 0.0001 were considered significant and reported as predicted ArcA binding sites.
Overnight cultures of strains 14028s wild type and ΔarcA were diluted (1:100) and cells were grown to OD600 ~ 0.4. At this point, H2O2 (1.0 mM) was added and cells were grown for 20 min. Control cells received no treatment. Experiments were performed in triplicate on different days. After treatment, 6 ml of cultures were withdrawn for each analysis and used for measurement of NADH, glutathione (GSH) and glutathione reductase (GR) activity. NADH was measured using commercially available kits by Abcam. The ratio between reduced glutathione and oxidized glutathione (GSH/GSSG) and GR activity were measured using commercially available kits by Cayman Chemicals. In all cases, measurements were performed following the instructions provided by the manufacturers without modifications.
Measurement of intracellular ROS was performed using the oxidant-sensitive probe H2DCFDA, as previously described, with minor modifications . Briefly, aerobically grown cells in LB at OD600 ~ 0.4 were incubated with 10 μM H2DCFDA. At 10 min intervals aliquots were taken, washed with 10 mM potassium phosphate buffer, pH 7.0, resuspended in the same buffer, and disrupted by sonication. Cell extracts (100 μl) were mixed with 1 ml phosphate buffer and fluorescence was measured using a TECAN Infinite 200 PRO Nanoquant microplate reader (excitation, 480 nm; emission, 520 nm). Emission values were normalized based on the bacterial concentration as determined by the Optical Density (OD) of the culture at 600 nm.
To analyze the role of ArcA in the transcriptional response to aerobiosis and H2O2, the ArcA regulon of S. Typhimurium was determined by microarray analysis. Expression profiles were measured from three independent samples of aerobically grown wild-type (14028s) and ΔarcA strains with or without 1 mM H2O2. After normalization, 3949 genes showed intensity values over the background in at least one array and were included in the analysis. The results were validated by randomly selecting eight genes and measuring the transcript levels by qRT-PCR (Additional file 1: Table S1). A statistically significant correlation was observed between microarray and qRT-PCR data (r2 = 0.7, p-value ≤ 0.0001), despite quantitative differences in the level of change, suggesting that the results obtained by microarray analysis reflect the actual changes in gene expression.
In the wild type strain, expression of 381 and 667 genes was up- or downregulated, respectively, in response to H2O2 under aerobic conditions (fold change ≥ 2, FDR q-value treatment ≤ 0.05, Additional file 2: Table S2). Several genes known to be upregulated by H2O2 and required for its resistance were among the upregulated genes in the wild type and ΔarcA strains, including katE, katG and mntH. A previous study investigated the effect of H2O2 on gene expression in a different S. Typhimurium strain, 4/74 . That study found 309 genes to be upregulated after H2O2 exposure, and 428 genes to be downregulated. The concurrence with our results in strain 14028s is about 30%: 119/381 upregulated 14028s genes and 191/667 downregulated 14028s genes had been found to be similarly regulated in strain 4/74. The observed differences in the number of genes differentially expressed might be explained by several factors including OD600 of treatment (0.4 vs 0.1), time of H2O2 challenge (20 min vs 12 min), threshold for considering a gene differentially expressed (fold change of ≥ 2 vs ≥ 3), and different S. Typhimurium strains used in the studies (14028s vs 4/74).
Role of ArcA during aerobic conditions
Pathways differentially regulated (q ≤ 0.25) by ArcA in response to H 2 O 2 and aerobiosis as determined by GSEA
Size of gene setA
Bacterial invasion of epithelial cells
Biosynthesis of siderophore group non-ribosomal peptides
Phosphotransferase system (PTS)
Bacterial secretion system
Cyanoamino acid metabolism
Ascorbate and aldarate metabolism
Amino sugar and nucleotide sugar metabolism
Fructose and mannose metabolism
Starch and sucrose metabolism
Cysteine and methionine metabolism
Role of ArcA in the response to H2O2 under aerobic conditions
It has been well established that an aerobically grown ΔarcA strain is sensitive to H2O2 treatment [7–10], however, the genes regulated by ArcA under this condition have not been determined. Our analysis shows that ArcA directly or indirectly regulates the expression of 292 genes in response to H2O2 in aerobically grown cells, 117 and 175 genes were up- or downregulated, respectively (Figure 1, Additional file 2: Table S2). Surprisingly, almost no correlation was observed between the genes regulated by ArcA in aerobiosis with or without H2O2: only 6 genes were upregulated under both conditions (Figure 1A), while 7 genes were downregulated (Figure 1B). Furthermore, comparison of the ArcA regulon in aerobiosis, anaerobiosis  and aerobiosis with H2O2 showed that no genes were up or downregulated in all three conditions (Figure 1A and B). This suggests that the genes regulated by ArcA in response to various stimuli are different and do hardly overlap (Figure 1), which underscores the importance and versatility of ArcA-mediated regulation.
To determine the pathways regulated by ArcA in response to H2O2 under aerobic conditions, the intensity values were treated as follows: (log2 14028s wild type H2O2 aerobic - log2 14028s wild type aerobic) - (log2 ΔarcA H2O2 aerobic - log2 ΔarcA aerobic). Therefore, in contrast to the pathways regulated by ArcA under aerobic conditions, the pathways positively regulated by ArcA in response to H2O2 under aerobic conditions have positive NES values, while the pathways negatively regulated by ArcA in response to H2O2 under aerobic conditions have negative NES values. Based on the transcriptomic data (Additional file 2: Table S2), GSEA deduced that 10 and 2 pathways were up- or downregulated, respectively, by ArcA in aerobically grown cells after H2O2 exposure (Table 1). The pathways deduced to be upregulated by ArcA in response to H2O2 are implicated in nucleotide and siderophore biosynthesis, central and glutathione metabolism, among others, while the pathways downregulated by ArcA were PTS and ABC transporters (Figure 2, Table 1). Interestingly, only one gene (ahpF) required for H2O2 degradation was upregulated by ArcA in aerobiosis after H2O2 treatment (Additional file 2: Table S2), suggesting that ArcA is not required for ROS scavenging. Of particular interest are the genes most upregulated by ArcA in aerobiosis with H2O2 in the pathways of nucleotide and glutathione metabolism, coding for the alternative ribonucleotide reductase (nrdEF) and glutathione reductase (gor). In addition, the gene coding for thioredoxin reductase (trxB), required for reduction of oxidized thioredoxin (Trx-[S]2), was also upregulated by ArcA after peroxide exposure. In E. coli, nrdEF is upregulated in response to H2O2[43, 44] and allows replication in iron-limiting conditions when manganese is present . Gor and TrxB are required for the turnover of oxidized glutathione (GSSG) and Trx-[S]2, respectively (reduction from GSSG to reduced glutathione (GSH), and Trx-[S]2 to reduced thioredoxin (Trx-[SH]2), respectively), which participate in the reduction of disulfide bonds . This suggests that in aerobically grown cells exposed to H2O2, ArcA regulates the GSH/GSSG and Trx-[S]2/Trx-[SH]2 ratio, modulating the redox status of the cell, and the expression of nrdEF.
Genes differentially expressed by ArcA under aerobic conditions with or without H 2 O 2 that have predicted ArcA binding sites
Fold change H2O2/control
Fold change control
5′ - 3′
DNA-binding transcriptional repressor MarR
putative periplasmic protein
putative methyl-accepting chemotaxis protein
short chain dehydrogenase
putative glutamic dehyrogenase-like protein
major sodium/proline symporter
secreted effector protein
putative transcriptional regulator
putative PTS permease
putative inner membrane protein
anti-RNA polymerase sigma 70 factor
putative cytoplasmic protein
putative RHS-like protein
cation transport regulator
respiratory NADH dehydrogenase 2
oligopeptide transport protein
bifunctional succinylornithine transaminase
Biochemical analysis of the ΔarcA strain
The microarray analysis predicted that in response to H2O2 under aerobic conditions, ArcA regulates the expression of genes implicated in GSH metabolism. It also predicted that in aerobiosis, ArcA regulates expression of genes coding proteins involved in glycolysis (Table 1 and Additional file 2: Table S2). To evaluate if the changes in gene expression correlated with changes in the products of these pathways, we determined the levels of GSH, glutathione reductase (GR) activity, NADH and total intracellular ROS in the wild type and ΔarcA strains in aerobiosis with and without H2O2.
The transcript levels of genes coding the pyruvate dehydrogenase complex (PDH), proteins of the payoff phase of glycolysis  and sugar uptake were higher in the aerobically grown ΔarcA mutant than in the wild type strain (Figure 2, Additional file 2: Table S2). This suggests that under aerobic conditions a ΔarcA strain has a higher flux through glycolysis, which in turn could result in higher levels of acetyl-CoA and an elevated NADH generation in the Krebs cycle. As predicted, the NADH/NAD+ ratio was significantly lowered in the aerobically grown wild type strain after peroxide treatment (Figure 3D), compared to untreated aerobically grown wild type cells. In the ΔarcA mutant, the NADH/NAD+ ratio was higher than in the wild type strain in aerobically grown cells before and after H2O2 treatment (Figure 3D). Although there was an overall decrease in the NADH/NAD+ ratio in the ΔarcA strain after H2O2 treatment, the ratio remained 2-fold higher than in wild type cells under aerobic conditions without H2O2 treatment.
In E. coli, one of the sources of O2- is oxidation of the respiratory electron transport chain and the conversion of NADH to NAD+. Since under aerobic growth conditions a ΔarcA strain has higher levels of NADH (Figure 3D) and ndh transcript than the wild type strain (Additional file 2: Table S2), we hypothesized that a ΔarcA mutant might present increased levels of total ROS. In agreement, in an aerobically grown ΔarcA strain, total ROS was increased as compared to the isogenic wild type strain under the same condition (Figure 3E), indicating that the absence of ArcA generates a metabolic imbalance which leads to increased levels of ROS.
In order to complement the ΔarcA mutation, we first evaluated the mechanism by which ArcA regulates gene expression in response to ROS. Our results show that in S. Typhimurium 14028s, arcA expression is not increased either with H2O2 or hypochlorous acid (Additional file 1: Figure S1A). In addition, the levels of ArcA also remained constant after exposure to both ROS (Additional file 1: Figure S1B). This suggests that rather than changes in expression, ArcA is activated in response to ROS, most likely by phosphorylation of residue D54. To test this hypothesis, the ΔarcA mutant strain was complemented in trans with the wild type gene and a version coding a substitution of residue D54 of ArcA (D54A), and the number of colony forming units (CFU/ml) was determined after H2O2 exposure. As predicted, only complementation with the wild type gene resulted in similar CFU/ml as in strain 14028s (Additional file 1: Figure S1C), however, there were also differences in the number of CFU/ml at the initial time points. This is most likely caused by increased levels of ArcA due to complementation with a high copy number vector. Since the effect of ArcA is pleiotropic and its levels remain constant throughout all stresses evaluated (Additional file 1: Figure S1 A and B), achieving wild type levels of ArcA is required to properly address its role in the response to ROS.
Role of ArcA in ROS scavenging
The S. Typhimurium genome codes for several genes that degrade H2O2 or organic hydroperoxide, including catalases (katG, katE and katN), alkyl hydroperoxide reductases (ahpCF and tsaA)  and a glutathione-dependent peroxidase (btuE) . Only ahpF and katE are predicted to be regulated by ArcA in aerobiosis with or without H2O2, respectively (Additional file 2: Table S2). Expression of ahpF and katE is also known to be regulated by RpoS [49, 50]. Neither katN nor sodA, previously described as members of the ArcA regulon under anaerobic conditions [8, 51], were found to be regulated by ArcA under aerobic conditions with or without H2O2 treatment. These results are in agreement with studies in E. coli that demonstrate that an arcA mutant does not show defects in H2O2 scavenging .
Role of ArcA in maintaining GSH and thioredoxin levels
ArcA positively regulates the expression of the genes gor (GR) and trxB (thioredoxin reductase) in aerobiosis with H2O2, but not without the toxic compound (Figure 2 and 4 Additional file 2: Table S2). However, the levels of GR activity were lower in the arcA mutant strain grown under aerobic conditions (Figure 3A), but not the levels of GSH turnover (Figure 3B). This suggests that there are other unidentified factors that alter GR activity in the arcA mutant grown under aerobic conditions, since there are no differences in the transcript levels of the gene gor between strains 14028s and ΔarcA (Additional file 2: Table S2). In addition, this indicates that the lower levels of GR activity in the arcA mutant grown under aerobic conditions are sufficient to cope with GSH turnover, and the effect is only evident when GSH oxidation is increased, as when cells are exposed to peroxide.
In E. coli, OxyR regulates gor expression , while the expression of trxB has not been determined under this condition. Two putative ArcA binding sites were predicted at the promoter region of trxB (Table 2). Glutathione and thioredoxin reductases are required to reduce GSSG and thioredoxin in a NADPH-dependant manner, which in their reduced form participate in the reduction of cellular disulfide bonds  and of oxidized glutaredoxin. An E. coli Δgor mutant has a slight sensitivity towards paraquat and cumene hydroperoxide , while in stationary phase a ΔtrxB strain shows H2O2 sensitivity . However, a double Δgor ΔtrxB mutant grows extremely poorly under aerobic conditions and presents increased alkaline phosphatase activity, indicative of increased disulfide bond formation, most likely due to increased ROS . Since an aerobically grown ΔarcA mutant treated with H2O2 has lower transcript levels of gor and trxB, lower GR activity and lower GSH levels (Figure 2 and 3A, B and C), this might result in increased disulfide bond formation, protein inactivation and contribute to the increased sensitivity towards ROS. Since GSH is abundant in the cell and is readily oxidized by H2O2, this leads to a decrease in the levels of reduced glutathione, shifting the target of oxidation from GSH to essential macromolecules, leading to cell death . This may occur earlier in a ΔarcA mutant, as its level of “protective” GSH is low, caused by decreased GR activity.
ArcA and nucleotide metabolism
The pathways that showed the highest changes in the ΔarcA mutant treated with H2O2 under aerobic conditions were purine and pyrimidine metabolism (Figure 4, Table 1). The major differences are found in the expression of the nrdAB and nrdEFHI operons, coding for aerobic and alternative aerobic ribonucleotide reductase, respectively. In E. coli and S. Typhimurium, NrdAB is indispensable for growth under aerobic conditions while NrdEF is not functional . In the aerobically grown wild type strain, nrdAB was repressed while nrdEF was up-regulated after H2O2 exposure, in agreement with studies in E. coli and S. Typhimurium 4/74 [41, 43], while the regulation was lost in the ΔarcA mutant under the same conditions (Additional file 2: Table S2). NrdEF is usually repressed by Fur. However, in response to H2O2, this Fur repression is abolished and the apoprotein form of IscR upregulates expression of the operon . This suggests that in response to H2O2 under aerobic conditions, ArcA may act together with Apo-IscR, up-regulating the nrdEFHI operon.
ArcA and carbon metabolism
Under aerobic conditions, the transcript levels of genes coding proteins of glycerolipid metabolism, glycolysis and the PDH complex were higher in the ΔarcA mutant than in the wild type strain (Figure 2 and 4, Additional file 2: Table S2). This suggests that the flux through glycolysis and the levels of acetyl-CoA could be increased in the ΔarcA strain. Two studies conducted in E. coli measured the flux through the PDH complex in a ΔarcA mutant under aerobic conditions with different results. One showed that there was an increase in the flux through the PDH complex  while in the other no differences were observed , although both studies determined that there was an increase in the flux through the TCA cycle. Our analysis showed that the NADH/NAD+ ratio was 2-fold higher in the aerobically grown ΔarcA mutant than in the wild type strain (Figure 3D). After H2O2 exposure, the NADH/NAD+ ratio decreased in the wild type and ΔarcA strain, but in the latter the levels remained higher than in the wild type strain under aerobic conditions (Figure 3D). Since NADH can reduce Fe3+ to Fe2+in vitro, and elevated NADH levels result in increased sensitivity towards H2O2, the higher basal levels of NADH in the ΔarcA mutant in aerobiosis and after H2O2 treatment may increase Fe+2 turnover, fueling the Fenton reaction (the formation of OH·, and Fe3+ from the nonenzymatic reaction of Fe2+ with H2O2) and leading to higher levels of ROS-derived damage.
In the respiratory chain, NADH dehydrogenase II (encoded by ndh) generates O2- and H2O2 by oxidation of its reduced FADH2 cofactor . In an aerobically grown ΔarcA strain, the levels of NADH and the ndh transcript (Additional file 2: Table S2) are higher than in the wild type strain under the same condition (Figure 3D). We therefore speculated that production of intracellular ROS might be increased. In agreement, a ΔarcA mutant presents statistically significant increased levels of total ROS as compared to the wild type strain 14028s (Figure 3E). These higher levels of ROS might present further disadvantages for the bacterium when exposed to H2O2. However, several other sources of intracellular ROS besides NADH dehydrogenase II may also contribute to the higher levels of ROS observed in the ΔarcA mutant, such as fumarate-reducing flavoenzymes .
We identified the ArcA regulon in S. Typhimurium under aerobic growth with and without H2O2, and show that ArcA coordinates a response that includes changes in cellular-, glutathione-, thioredoxin-, NADH- and glycerolipid metabolism. These changes contribute to H2O2 resistance by modulating the reducing potential of the cell.
EHM and CPS conceived the project. EHM and PD conducted the analysis of microarray data and prediction of regulated pathways. EHM, BC and ILC performed the experiments. FG, RL and SP conducted partial data analysis. EHM, SP, MM and CPS wrote the paper. All authors read and approved the final manuscript. The authors declare no conflict of interest.
This work was supported by grants from FONDECYT #1120384 (to CPS), Universidad Andres Bello DI-34-11/R (to CPS), DI-24-12/I (to EHM) and DI-19-12/I (to BC). EHM and BC received doctoral fellowships by CONICYT and MECESUP UAB0802 additionally to EHM. The authors wish to thank Dr. Claudio Vásquez for critical reading the manuscript.
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